ePRO Resources

  1. Simplify Today. Transform For The Future. 10/25/2023

    Maximize efficiency today with a cloud-based user-friendly platform that seamlessly adapts to the future of phase 1-3 trials. Watch to see how Zelta can help.

  2. Designing ePRO and eConsent Solutions that Participants and Sites Want 10/26/2022

    Participant-focused eClinical technologies offer significant potential to decrease paper-based processes and improve end-user experiences in collecting patient-reported outcomes (PRO) and informed consent, but many users continue to experience rigid technology, complicated hardware provisioning processes, and clunky implementations that leave sponsors, CROs and sites questioning the value. 

  3. Still Using Paper Diaries To Capture PRO Data? Read This. 1/8/2024

    Access real-world examples of how electronic patient-reported outcome measures (PROMs) optimize data quality and reliability and improve the statistical power of trial data.

  4. Exploring The Potential Of Non-Consumer Smartphones In Clinical Trials 4/17/2024

    We selected and evaluated a non-consumer device, to explore its potential as a reliable tool for home-based ePRO measure administration. Here’s what we learned from this usability testing. 

  5. Simplifying ePRO Data Collection 10/4/2024

    The Bring Your Own Device (BYOD) model, supported by Trialkit, is an innovative approach in clinical trials that allows participants to use personal smartphones or tablets for data collection.

  6. C3 Summit Recap: Shaping The Future Of eCOA/ePRO Highlights 2/10/2022

    Understand how the rapid shift to decentralized clinical trials required pharma companies and CROs to adapt data capture techniques quickly while remaining compliant with local regulations.

  7. Leveraging Tech And Clinician Review To Improve Risk Detection 10/19/2023

    Learn why neuroscience therapy developers should start adopting strategies to improve data quality and assess responses using a combination of technology and expert clinician review.

  8. Overcoming Oncology Trial Challenges With ePRO Solutions 5/16/2023

    Discover effective strategies and solutions to overcome challenges in oncology studies and how to optimize trial design, patient recruitment, data management, and regulatory compliance.

  9. Mitigating The Risks Of Long-Term Oncology eCOA Clinical Trials 6/23/2022

    This article digs into the specific complexities of long oncology clinical trials and describes relevant solutions to manage the risks regarding patient compliance, clinical project teams, and clinical sites.

  10. Why eConsent Makes Such A Difference In Patient Adherence And Engagement 6/6/2022

    Explore how consent is a critical step that can greatly influence patient enrollment, adherence and retention in the trial.